Study Comparing Two Administration Pathways for Adenosine During Microvascular Function Assessment
- Conditions
- Microvascular Coronary Artery Disease
- Interventions
- Diagnostic Test: microvascular function assessment
- Registration Number
- NCT06269874
- Lead Sponsor
- Johannes Gutenberg University Mainz
- Brief Summary
The aim of this study is to investigate the agreement and reproducibility between intravenous and intracoronary adenosine administration during invasive assessment of microvascular function.
Goals of this study are:
1. Agreement and reproducibility between intravenous and intracoronary adenosine administration in the IMR (Index of microvascular resistance) value.
2. Agreement and reproducibility of FFR(fractional flow reserve), CFR (coronary flow reserve), MRR (microvascular resistance reserve), RRR (resistive reserve ratio) and reproducibility of each of these as compared with CFRabs (absolute coronary flow).
3. Time required for IMR measurements
- Detailed Description
The study is a single-center randomized, cross-over controlled, open label trial to investigate the reproducibility and agreement between intravenous and intracoronary adenosine administration during invasive assessment of microvascular function.
The primary analysis will be on the per-protocol population (i.e. including all patients who are not protocol violators).
Primary endpoint:
1. Agreement and reproducibility between intravenous and intracoronary adenosine administration in the IMR value.
Secondary endpoints:
1. Agreement and reproducibility of FFR, CFR, MRR, RRR and reproducibility of each of these as compared with CFRabs.
2. Time required for IMR measurements
3. Presence and severity of angina, assessed by SAQ(Seattle Angina Questionnaire)-7
4. Assessment of safety: Presence and severity of AV( atrioventricular) block, dyspnea, flush
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 40
- Chronic coronary syndrome (including patients with anginal equivalents).
- Indication to cardiac catheterization;
- Indication to the assessment of microvascular function (note: patients will be asked for participation and consented prior to the first measurement of microvascular function, which will be conducted as per clinical indication)
- Willingness to participate and ability to understand, read and sign the informed consent
- Age>18 years
- Age <18 years
- Bronchial asthma, COPD (chronic obstructive pulmonary disease)
- Secondary or tertiary atrioventricular block without prior pacemaker implantation
- Previous CABG (coronary artery bypass graft) with patent grafts to the left anterior descending coronary
- Epicardial coronary disease (FFR <0.80 with evidence of a focal stenosis) in the left anterior descending territory
- Inability to provide informed consent
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Intravenous Adenosine microvascular function assessment Invasive microvascular function assessment will be conducted by administering intravenous hyperemic agent adenosine. Intracoronary Adenosine microvascular function assessment Invasive microvascular function assessment will be conducted by administering intracoronary hyperemic agent adenosine.
- Primary Outcome Measures
Name Time Method Agreement between intravenous and intracoronary adenosine responses (IMR) 6 months Agreement and reproducibility between IMR (index of microvascular resistance) obtained with intravenous and intracoronary adenosine administration during invasive assessment of microvascular function as assessed by Cohen´s Kappa, intraclass correlation coefficient and Bland-Altman analysis.
- Secondary Outcome Measures
Name Time Method Time required for IMR measurements 6 months Comparison of time required for measuring IMR between intracoronary and intravenous adenosine administration
Agreement between secondary parameters and reproducibility as compared with absolute 6 months Agreement and reproducibility between secondary parameters (MRR, RRR, Pd/Pa, FFR, CFR, Ach-IMR) obtained with intravenous and intracoronary adenosine administration during invasive assessment of microvascular function as assessed by Cohen´s Kappa, intraclass correlation coefficient and Bland-Altman analysis.
Trial Locations
- Locations (1)
Center of Cardiology, Cardiology I, university hospital Mainz
🇩🇪Mainz, Rheinland-Pfalz, Germany